Variant #0001013353 (NC_000001.10:g.93300404T>A, NM_000969.3:c.258T>A (RPL5))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.93300404T>A
DNA change (hg38) -
Published as RPL5(NM_000969.5):c.258T>A (p.Y86*)
ISCN -
DB-ID FAM69A_000016
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-10-29 20:49:11 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RPL5 NM_000969.3 +/. - c.258T>A r.(?) p.(Tyr86*)
FAM69A NM_001006605.4 +/. - c.*8536A>T r.(=) p.(=)


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